Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

Mutation

Drugs
Downloads

id	TP53	VariantID	Class	ConseqType	AA	AAcoord	sift_sort	SIFT	polyphen_sort	polyphen_class	PolyPhen	cadd_sort	cadd_class	CADD
23061	MLL2	rs1255523264	SNP	missense variant	P/S	4601	81	0.08	1	benign	0	13001	likely benign	13
23062	MLL2	rs1255523264	SNP	missense variant	P/A	4601	101	0.1	1	benign	0	11001	likely benign	11
23063	MLL2	rs577303074	SNP	missense variant	A/V	4599	801	0.8	1	benign	0	8001	likely benign	8
23064	MLL2	rs201879072	SNP	missense variant	A/T	4599	411	0.41	1	benign	0	12001	likely benign	12
23065	MLL2	rs545972414	SNP	missense variant	A/P	4594	1	0	544	possibly damaging	0.543	22001	likely benign	22
23066	MLL2	rs1425274289	SNP	missense variant	G/E	4593	1	0	662	possibly damaging	0.661	25001	likely benign	25
23067	MLL2	rs1044708169	SNP	missense variant	Q/H	4588	51	0.05	1	benign	0	17001	likely benign	17
23068	MLL2	rs760847881	SNP	missense variant	Q/R	4588	121	0.12	1	benign	0	21001	likely benign	21
23069	MLL2	rs1341876968	SNP	missense variant	N/Y	4586	1	0	242	benign	0.241	22001	likely benign	22
23070	MLL2	rs766593097	SNP	missense variant	C/W	4583	21	0.02	316	benign	0.315	23001	likely benign	23

Left 2306 2307 2308